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C Scharfe

Showing results (1-10 of 11) with videos related to

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Cytogenetics and Cell Genetics|January 1, 1997
Report of the second international workshop on human chromosome 10 mapping 1997T Meitinger, C Scharfe, K Call, et al.
Nucleic Acids Research|December 31, 2005
MitoP2: the mitochondrial proteome database--now including mouse dataH Prokisch, C Andreoli, U Ahting, et al.
Nucleic Acids Research|December 19, 2003
MitoP2, an integrated database on mitochondrial proteins in yeast and manC Andreoli, H Prokisch, K Hörtnagel, et al.
Journal of Medical Genetics|September 9, 2000
A novel mutation in the thiamine responsive megaloblastic anaemia gene SLC19A2 in a patient with deficiency of respiratory chain complex IC Scharfe, M Hauschild, T Klopstock, et al.
Human Molecular Genetics|November 18, 1998
Diabetes insipidus, diabetes mellitus, optic atrophy and deafness (DIDMOAD) caused by mutations in a novel gene (wolframin) coding for a predicted transmembrane proteinT M Strom, K Hörtnagel, S Hofmann, et al.
Nucleic Acids Research|December 10, 1998
MITOP: database for mitochondria-related proteins, genes and diseasesC Scharfe, P Zaccaria, K Hoertnagel, et al.
Journal of Medical Genetics|October 5, 2001
Frequency of mitochondrial transfer RNA mutations and deletions in 225 patients presenting with respiratory chain deficienciesM Jaksch, S Kleinle, C Scharfe, et al.
Journal of Medical Genetics|October 22, 2003
A tRNA(Ala) mutation causing mitochondrial myopathy clinically resembling myotonic dystrophyR Horváth, H Lochmüller, C Scharfe, et al.
Nucleic Acids Research|December 11, 1999
MITOP, the mitochondrial proteome database: 2000 updateC Scharfe, P Zaccaria, K Hoertnagel, et al.
Journal of Medical Genetics|November 5, 2002
Childhood onset mitochondrial myopathy and lactic acidosis caused by a stop mutation in the mitochondrial cytochrome c oxidase III geneR Horváth, C Scharfe, M Hoeltzenbein, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Cytogenetics and Cell Genetics|January 1, 1997
Report of the second international workshop on human chromosome 10 mapping 1997T Meitinger, C Scharfe, K Call, et al.
Nucleic Acids Research|December 31, 2005
MitoP2: the mitochondrial proteome database--now including mouse dataH Prokisch, C Andreoli, U Ahting, et al.
Nucleic Acids Research|December 19, 2003
MitoP2, an integrated database on mitochondrial proteins in yeast and manC Andreoli, H Prokisch, K Hörtnagel, et al.
Journal of Medical Genetics|September 9, 2000
A novel mutation in the thiamine responsive megaloblastic anaemia gene SLC19A2 in a patient with deficiency of respiratory chain complex IC Scharfe, M Hauschild, T Klopstock, et al.
Human Molecular Genetics|November 18, 1998
Diabetes insipidus, diabetes mellitus, optic atrophy and deafness (DIDMOAD) caused by mutations in a novel gene (wolframin) coding for a predicted transmembrane proteinT M Strom, K Hörtnagel, S Hofmann, et al.
Nucleic Acids Research|December 10, 1998
MITOP: database for mitochondria-related proteins, genes and diseasesC Scharfe, P Zaccaria, K Hoertnagel, et al.
Journal of Medical Genetics|October 5, 2001
Frequency of mitochondrial transfer RNA mutations and deletions in 225 patients presenting with respiratory chain deficienciesM Jaksch, S Kleinle, C Scharfe, et al.
Journal of Medical Genetics|October 22, 2003
A tRNA(Ala) mutation causing mitochondrial myopathy clinically resembling myotonic dystrophyR Horváth, H Lochmüller, C Scharfe, et al.
Nucleic Acids Research|December 11, 1999
MITOP, the mitochondrial proteome database: 2000 updateC Scharfe, P Zaccaria, K Hoertnagel, et al.
Journal of Medical Genetics|November 5, 2002
Childhood onset mitochondrial myopathy and lactic acidosis caused by a stop mutation in the mitochondrial cytochrome c oxidase III geneR Horváth, C Scharfe, M Hoeltzenbein, et al.
Pageof 2